Arthrogryposis multiplex congenita

From BugSigDB


Arthrogryposis multiplex congenita (AMC) is a group of disorder characterized by congenital limb malformation. It manifests by non-progressive multiple joint contractures that incorporate muscle weakness and fibrosis, resulting from a large number of disorders.
Aliases
  • AMC
  • Amyoplasia congenita
  • amyoplasia congenita
  • arthrogryposis multiplex congenita
  • Arthromyodysplasia congenita
  • Congenital amyoplasia
  • congenital amyoplasia
  • Congenital arthromyodysplasia
  • congenital arthromyodysplasia
  • fibrous ankylosis of multiple joints
  • Guerin-Stern syndrome
  • Guérin-Stern syndrome
  • Multiple congenital arthrogryposis
  • multiple congenital arthrogryposis
  • Myodysplasia
  • myodysplasia
  • myodystrophia fetalis deformans
  • Otto syndrome
  • rocher-Sheldon syndrome
  • Rossi syndrome